Mckesson recalls Olanzapine 10mg single-dose vials due to temperature abuse risks. Affected products may have been shipped with improper temperature control.
cGMP deviations: Temperature abuse
Mckesson is recalling Olanzapine 10mg single-dose vials that were manufactured by Auromedics Pharma LLC. The recall is due to temperature abuse risks during storage or shipping, which could lead to unsafe drug conditions.
Temperature abuse during storage or shipping could cause the medication to become unstable. This might lead to improper drug conditions that could affect safety when used.
Prescription patients using Olanzapine 10mg vials from Auromedics Pharma LLC. Patients who received these vials through McKesson Medical-Surgical pharmacies are most at risk.
Check for the product name 'Olanzapine single dose vial Lyophilized, 10 mg, Rx only' with manufacturer Auromedics Pharma LLC and NDC# 55150-0308-01. Products were distributed by McKesson Medical-Surgical starting from the date mentioned in the recall notice.
Look for the product name, manufacturer, and NDC number to confirm if your vial is affected.
The recall is due to temperature abuse risks during storage or shipping, which could cause the medication to become unstable.
Check for the product name 'Olanzapine single dose vial Lyophilized, 10 mg, Rx only' with manufacturer Auromedics Pharma LLC and NDC# 55150-0308-01.
The recall notice does not specify a remedy or action for affected products.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1005-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1005-2022 from Mckesson Medical-Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.